Canonical Allele Identifier: CA506095408

Gene: ANKLE1

Linked Data

• MyVariant Identifiers: chr19:g.17394035C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17283226C>A , CM000681.2:g.17283226C>A	GRCh38
NC_000019.9:g.17394035C>A , CM000681.1:g.17394035C>A	GRCh37
NC_000019.8:g.17255035C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404085.7:c.462C>A MANE Select	ENSP00000384008.3:p.Thr154=
ENST00000404261.9:c.462C>A	ENSP00000384753.6:p.Thr154=
ENST00000594072.6:c.462C>A	ENSP00000468845.4:p.Thr154=
ENST00000651416.1:n.679C>A
ENST00000652132.1:c.429C>A	ENSP00000498416.1:p.Thr143=
ENST00000394458.7:c.624C>A	ENSP00000377971.4:p.Thr208=
ENST00000404085.5:c.*361C>A	ENSP00000384008.2:n.*361C>A
ENST00000404261.8:c.624C>A	ENSP00000384753.5:p.Thr208=
ENST00000594072.5:c.624C>A	ENSP00000468845.3:p.Thr208=
ENST00000596626.1:n.575C>A
ENST00000598347.2:c.464C>A
NM_001278443.1:c.591C>A	NP_001265372.1:p.Thr197=
NM_001278444.1:c.624C>A	NP_001265373.1:p.Thr208=
NM_001278445.1:c.528C>A	NP_001265374.1:p.Thr176=
NM_152363.5:c.624C>A	NP_689576.5:p.Thr208=
NR_103530.1:n.738C>A
NM_001278443.2:c.429C>A	NP_001265372.2:p.Thr143=
NM_001278444.2:c.462C>A	NP_001265373.2:p.Thr154=
NM_001278445.2:c.420C>A	NP_001265374.2:p.Thr140=
NM_152363.6:c.462C>A MANE Select	NP_689576.6:p.Thr154=
NR_103530.2:n.482C>A